|
HS Code |
234443 |
| Product Name | 6-Amino-3-cyano-2-methylpyridine |
| Cas Number | 22398-80-7 |
| Molecular Formula | C7H7N3 |
| Molecular Weight | 133.15 |
| Appearance | Off-white to pale yellow powder |
| Melting Point | 117-121°C |
| Purity | ≥98% |
| Boiling Point | No data available |
| Solubility | Slightly soluble in water |
| Density | No data available |
| Storage Temperature | Store at room temperature |
| Synonyms | 2-Methyl-6-aminonicotinonitrile |
| Smiles | CC1=NC=C(C#N)C(N)=C1 |
| Inchi | InChI=1S/C7H7N3/c1-5-6(4-8)2-3-7(9)10-5/h2-3H,9H2,1H3 |
As an accredited 6-AMINO-3-CYANO-2-METHYLPYRIDINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g white plastic bottle, clearly labeled with "6-AMINO-3-CYANO-2-METHYLPYRIDINE," hazard symbols, and storage instructions, tightly sealed. |
| Container Loading (20′ FCL) | 20′ FCL loaded with 6-AMINO-3-CYANO-2-METHYLPYRIDINE, securely packed in drums/cartons, compliant with safety and transport regulations. |
| Shipping | 6-Amino-3-cyano-2-methylpyridine is shipped in tightly sealed containers, protected from light and moisture. The chemical should be handled according to standard laboratory safety protocols, with labeling for hazardous material if applicable. Shipping complies with regulatory requirements for transport of chemicals and may require accompanying safety data sheets (SDS). |
| Storage | **6-Amino-3-cyano-2-methylpyridine** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect the chemical from light, moisture, and sources of ignition. Proper chemical labeling is required, and access should be restricted to trained personnel. Use secondary containment to prevent spills or accidental release. |
| Shelf Life | The shelf life of 6-amino-3-cyano-2-methylpyridine is typically 2–3 years when stored in a cool, dry, tightly sealed container. |
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Purity 99%: 6-AMINO-3-CYANO-2-METHYLPYRIDINE with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and low impurity levels. Melting Point 118°C: 6-AMINO-3-CYANO-2-METHYLPYRIDINE with melting point 118°C is used in organic crystal development, where it provides consistent phase transition control. Molecular Weight 135.15 g/mol: 6-AMINO-3-CYANO-2-METHYLPYRIDINE with molecular weight 135.15 g/mol is used in analytical reference standards, where it offers reliable calibration accuracy. Particle Size <50 µm: 6-AMINO-3-CYANO-2-METHYLPYRIDINE with particle size below 50 micrometers is used in fine chemical formulations, where it promotes homogeneous dispersion. Stability Temperature up to 120°C: 6-AMINO-3-CYANO-2-METHYLPYRIDINE with stability temperature up to 120°C is used in heated batch reactions, where it maintains structural integrity. Solubility in DMSO 30 mg/mL: 6-AMINO-3-CYANO-2-METHYLPYRIDINE with solubility in DMSO at 30 mg/mL is used in solution-based assays, where it enables accurate dosing and reproducibility. Residual Moisture ≤0.5%: 6-AMINO-3-CYANO-2-METHYLPYRIDINE with residual moisture less than or equal to 0.5% is used in sensitive dehydrated formulations, where it prevents hydrolytic degradation. Optical Purity ≥98%: 6-AMINO-3-CYANO-2-METHYLPYRIDINE with optical purity greater than or equal to 98% is used in chiral synthesis routes, where it reduces the need for downstream purification. |
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Some chemicals may seem like just another name and number on a list, but anyone who has stepped foot into a research lab knows differently. 6-Amino-3-cyano-2-methylpyridine stands out for researchers and professionals looking for real solutions in organic synthesis, pharmaceutical development, and specialty material production. As the demand for precision and better results grows, more attention turns to specialty building blocks like this one—not for the sake of novelty, but for the way these compounds help craft genuine scientific progress. Not all chemicals can claim to be both versatile and reliable; this one manages both, thanks to a straightforward structure and a set of properties that make a difference in practice.
6-Amino-3-cyano-2-methylpyridine isn’t the most glamorous molecule at a glance. Its six-membered pyridine ring, methyl group at the 2-position, amino group at the 6-position, and cyano group at the 3-position team up to give it a clear edge in lab-based work. I still remember my first graduate project trying to introduce a cyano group into a heterocycle—nothing seemed to go right until I found a starting material that had the right balance of nucleophilic and electrophilic spots. This compound brings that to the table, and you notice its value after working with less cooperative analogs.
The molecule’s unique substitution pattern doesn’t exist for complexity’s sake. Each functional group sits in a position that allows for selective modification. In practice, that opens doors: attaching a bulky group on the nitrogen, building out from the cyano for new ring systems, or tweaking electronic properties for better biological interaction. Some competitors have overlapping properties, but not every alternative lets you dial in reactivity and selectivity so precisely.
It’s easy to underestimate the challenges involved in building complex molecules. Many drugs and advanced materials start with reliable building blocks that can take a beating during several tough reaction steps. In the lab, you quickly see which compounds fall apart or don’t react as you need them to; 6-amino-3-cyano-2-methylpyridine holds up well, taking on substitutions, reductions, and cyclizations without the drama or unpredictable byproducts you might get from other pyridine derivatives.
Pharmaceutical researchers lean on it for scaffold construction. The cyano group gives a handle for conversion to amides, carboxylic acids, or other valuable pieces. Medicinal chemists value being able to build on that core, trying new substitutions that might tweak how a molecule interacts with its biological target, hopes for better results in clinical screens. Having worked beside colleagues screening analog series, I’ve seen how a material like this can shave weeks from a development timeline. No one wants to re-route a synthesis mid-project if a starting material fails; this one helps avoid those headaches.
In agrochemical R&D, similar arguments hold. When designing actives against plant pathogens or pests, researchers chase new chemotypes—a fresh backbone can beat resistance or open up new patentable space. The nitrogen and cyano cornerstones of this molecule provide launching points for optimization. Real-world impact plays out not just in patents, but in how quickly a team can hit a project milestone thanks to a solid starting point.
Outside pharmaceuticals, 6-amino-3-cyano-2-methylpyridine lands in specialty material applications, with the pyridine core offering the right balance of rigidity and tunable activity. With the boom in organic electronics and functional dyes, scientists prize molecules that can serve as intermediates for advanced ring systems or that contribute to electron-rich environments for charge transfer. Here, the amino and cyano groups can orient the compound for the next reaction—whether forming a polymer precursor or a ligand for metal complexes with unique luminescent properties.
Fieldwork has shown that subtle tweaks on pyridines, especially the way functional groups are spaced, often make or break new material candidates. Many times, our team saw alternatives falter—too much instability, awkward reaction conditions, or simply a lack of flexibility in subsequent chemistry. 6-amino-3-cyano-2-methylpyridine doesn’t waste anyone’s time, since the groups are positioned to allow extensions in multiple directions without harsh conditions or toxic reagents, a big plus when scaling up to pilot batches.
Another factor some overlook boils down to experience on the bench. You may find all sorts of pyridine intermediates in catalogs, but not every sample comes with the purity or consistency you expect. Researchers who’ve lived through erratic results or had to spend mornings chasing impurities know the pain. High-purity batches of 6-amino-3-cyano-2-methylpyridine—often above 98% by HPLC—reduce this hassle. Less time with column chromatography, more time pushing projects forward.
Supplying partners who understand the realities of lab life matters, too. Stable packaging, documented batch quality, and ready shipping timelines help labs avoid the traps of spoiled or degraded intermediates. In sourcing chemicals over years, I’ve learned to value suppliers who take this as seriously as the scientists do. It keeps research on schedule, a detail that separates reliable progress from constant troubleshooting.
Anyone working with pyridines will notice how minor modifications in structure lead to big changes in chemical behavior. Substituents make the difference between a five-minute separation and a miserable afternoon, or a reliable reaction and low conversion. Many alternatives—such as unsubstituted aminopyridines or standard cyanopyridines—don’t offer the same blend of reactivity and stability. Unsubstituted analogs often lack specificity in downstream chemistry. In contrast, the methyl group at position 2 on this molecule tweaks the electron density enough to influence both selectivity and solubility.
Some pyridines bring reactivity but not control; others endure harsh steps, but don’t play well with downstream transformations. With 6-amino-3-cyano-2-methylpyridine, you notice the difference in both settings—productive yields in substitutions or reductions, and cleaner separations during purification. From my own trials, few other compounds combine these three groups in a way that’s as enabling or robust under real-world lab conditions.
Those responsible for laboratory or pilot-plant environments know that availability and utility only go so far without safety and responsible management. 6-Amino-3-cyano-2-methylpyridine benefits from having a manageable risk profile compared to many more reactive or less predictable intermediates. While safety data drives protocols—proper ventilation, personal protective equipment, and secure storage—the compound usually meets hazard expectations for its chemical class without introducing surprise liabilities.
Teams looking to minimize environmental impact appreciate that it doesn’t require exotic solvents or aggressive conditions for standard transformations. When colleagues switched out more problematic intermediates, the net reduction in hazardous waste and nuisance disposal was real. Attention to closed-system handling, solvent minimization, and batch tracking keeps this chemical a reliable option for firms developing greener workflows.
Working on cross-company collaborations, I’ve seen first-hand how a well-chosen building block can skip months of trial-and-error. Synthesis teams often share stories about bottlenecks: materials that react unpredictably, introduce side products, or simply cost too much to purchase at scale. In one particular project aimed at creating kinase inhibitors, a group struggled for months with an unstable intermediate. The switch to 6-amino-3-cyano-2-methylpyridine, thanks to its convenient substitution points, allowed for a more straightforward cyclization, which shortened the route by two steps and produced higher purity in the final compound. These aren’t isolated incidents.
In material science collaborations, choosing the wrong starting point often sets entire programs back due to solubility or reactivity concerns. Colleagues in the dye and pigment sector have noticed that introducing new functional groups via this compound, especially for extended conjugation systems, provides access to shades and performance not achieved with less versatile analogs. Whenever a discussion about new candidate intermediates comes up, the track record of this molecule provides a genuine sense of reassurance in meetings. Nobody wants to throw good money after bad on chemicals that just don’t perform reliably.
Scaling laboratory reactions to pilot or full production isn’t just an exercise in mixing bigger batches; chemical quirks get magnified with volume. Some intermediates behave perfectly in flasks but refuse to scale—byproducts increase, crystallization problems pop up, or batch-to-batch variations erode consistency. 6-Amino-3-cyano-2-methylpyridine stands out for its predictability from gram-scale research all the way to multi-kilogram manufacturing. Recrystallization or basic distillation usually gives a clean, free-flowing solid with minimal fuss.
Production staff and managers I’ve worked with value materials that reduce the need for extensive purification or rework. Less energy spent correcting issues means lower operational costs and quicker delivery to customers. The feedback cycle between process chemists and manufacturing teams is much healthier when you can trust an intermediate to act as expected in each batch. In my own experience, compounds like this build the foundation for a better, more flexible manufacturing process.
Wide adoption of 6-amino-3-cyano-2-methylpyridine across several regions reflects its fit with global regulatory standards. Whether one works in the European Union, North America, or Asia, sourcing partners ensure compliance with industry norms on impurities, documentation, and transport safety. Project teams benefit from clear batch histories and certificates of analysis, bypassing the wild variability seen in more obscure intermediates. In recent years, as supply chains have seen more scrutiny, reliable sources for this compound have kept projects on track even when other materials fell into short supply or ran into regulatory snags.
Compatibility with mainstream analytical methods—NMR, IR, mass spectrometry—makes quality verification straightforward, a real boost for teams who can’t spare time on ambiguous or unexpected results. In daily practice, this means smoother regulatory filings and fewer detours into analytical troubleshooting.
After years spent comparing hundreds of intermediates across pharma, electronics, and materials fields, a pattern emerges. The intermediates that stick around in lab catalogs and on production lines deliver three things: consistent availability, robust performance in a range of reactions, and manageable safety handling. 6-Amino-3-cyano-2-methylpyridine ticks these boxes as well as any compound I’ve encountered.
In my experience, frustrations in research often come from subtle mismatches—a molecule that should react doesn’t, or a promising intermediate fails in scaling. Here, blends of functional groups help sidestep these issues: the amino group opens up coupling options, the cyano offers a hook for further transformation, the methyl shifts solubility and influences regioselectivity. The payoff isn’t just in chemical yields, but also in time saved and confidence gained through each step of a synthesis or process.
Chemical innovation doesn’t happen in a vacuum. The best tools aren’t just new; they’re the ones that let professionals get real work done, under deadlines and budget pressures, without endless retrials. This compound lives up to that standard in the hands of those who know what counts: clear reactivity, solid supply chains, and the flexibility to serve several demanding fields at once.
No tool solves every challenge, and even reliable intermediates have their limits. Some transformation routes using 6-amino-3-cyano-2-methylpyridine still depend on tuning solvents or catalysts to steer selectivity and conversion. In certain downstream uses, solubility ceilings might pop up earlier than hoped, nudging chemists to explore salt forms or co-solvent systems. These aren’t insurmountable; most research and production teams tackle such issues with incremental adjustments and feedback from analytic data.
In large-scale runs, any intermediate can be a source of waste or emissions if the process doesn’t dial in. The best results come from cross-talk between research, process development, and operations staff—a habit of open reporting on real yields, observed hazards, and practical workarounds. Not every new intermediate achieves that level of buy-in, but experience shows that established compounds like this one draw more creative solutions and peer-shared tips over time. Many process tweaks that keep operations safer or more sustainable start with candid feedback on the bench.
Where future improvements might develop, green chemistry remains a promising focus. Sourcing partners may move toward greener precursors, solvent recovery, or more energy-efficient production routes. Research teams can push efficiency higher by pairing this intermediate with milder reagents or continuous-flow technologies, strategies that cut both cost and risk. Industry knowledge grows fastest when specialists share results openly—both the wins and the challenges that need creative fixes.
Trust matters in chemistry—between researchers, suppliers, and the wider community that depends on reliable products. Every sample of 6-amino-3-cyano-2-methylpyridine sent to a workplace carries expectations not just for technical performance but for responsible sourcing and transparent documentation. As open access to safety data improves, labs school newcomers not just on proper technique but on sourcing from partners committed to safe, sustainable, and steadily supplied materials.
Practical experience trumps catalog promises. Colleagues in both startups and multinational research teams attest to the outsize impact a reliable intermediate can have, whether it’s launching a promising new drug candidate or hitting a milestone on a new OLED material. The difference so often comes down to having the right building block at the right time—an advantage this compound offers to researchers across the globe.
Whether the project is about synthesizing leads for a disease target, developing next-generation functional polymers, or simply staying on top of project timelines, 6-amino-3-cyano-2-methylpyridine brings proven value. It anchors workflows that emphasize safety, predictability, and freedom to test new concepts with fewer unpleasant surprises along the way.
I’ve seen continuous improvements arise in both small and large organizations by prioritizing intermediates that build confidence from the bench to the boardroom. For many, this pyridine derivative represents one of the go-to choices when the balance between reactivity, safety, and efficiency really counts. That track record explains why it keeps finding its way into published protocols and standard operating procedures, not just in academia but across the high-stakes worlds of pharmaceuticals, crop science, and advanced materials. As the demands on chemists keep rising and the push for better, safer, more responsible products continues, molecules like this will keep earning their place in the toolbox—not through hype, but through reliable, hands-on results, shaped by a long line of practical experience.